| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96870072-96870134 | Common:1; Rare:17 | ||||
| chr2:97645870-97646215 | Common:3; Rare:101 | ||||
| chr2:97663982-97664294 | Rare:88 | ||||
| chr2:98608412-98608648 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr2:99141147-99141435 | Common:1; Rare:101 | ||||
| chr2:99141523-99141576 | Rare:27 | ||||
| chr2:99154862-99155094 | Common:3; Rare:95; Clinvar (benign):3 | ||||
| chr2:99180853-99181250 | Common:2; Rare:128 | ||||
| chr2:99181319-99181555 | Rare:49 | ||||
| chr2:99336242-99336428 | Common:1; Rare:57 | ||||
| chr2:99337310-99337582 | Rare:102 | ||||
| chr2:99489935-99490350 | Common:2; Rare:170 | ||||
| chr2:100562896-100563070 | Rare:59 | ||||
| chr2:101151134-101151203 | Rare:12 | ||||
| chr2:101151347-101151587 | Common:3; Rare:76 |